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Key Documents

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45371

Supelco

Carboxine

PESTANAL®, analytical standard

Sinônimo(s):

5,6-Dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide, Carbathiine

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About This Item

Fórmula empírica (Notação de Hill):
C12H13NO2S
Número CAS:
5234-68-4
Peso molecular:
235.30
Beilstein:
983249
Número CE:
226-031-1
Número MDL:
MFCD00055403
Código UNSPSC:
41116107
ID de substância PubChem:
329756679
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

CC1=C(SCCO1)C(=O)Nc2ccccc2

InChI

1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)

chave InChI

GYSSRZJIHXQEHQ-UHFFFAOYSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informações legais

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Palavra indicadora

Warning

Frases de perigo

H302,H317,H373,H410

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2

Órgãos-alvo

Kidney

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

212.0 °F - closed cup

Ponto de fulgor (°C)

100 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCC3071
BCBT8120
BCBT3580
SZBG069XV
SZBC023XV

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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Supelco

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Sigma-Aldrich

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Rotenone

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Sigma-Aldrich

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Sreedhar Kilaru et al.
Current genetics, 55(5), 543-550 (2009-07-29)
Dominant selectable markers are beneficial for transformation of many fungi, particularly those model species where repeated transformations may be required. A carboxin resistance allele of the Coprinopsis cinerea sdi1 gene, encoding the iron-sulphur protein subunit of succinate dehydrogenase, was developed
Lars Hederstedt
Biochimica et biophysica acta, 1553(1-2), 74-83 (2002-01-23)
An overview of the present knowledge about succinate:quinone oxidoreductase in Paracoccus denitrificans and Bacillus subtilis is presented. P. denitrificans contains a monoheme succinate:ubiquinone oxidoreductase that is similar to that of mammalian mitochondria with respect to composition and sensitivity to carboxin.
Akinori Ando et al.
Current genetics, 55(3), 349-356 (2009-05-26)
The sdhB gene encoding an iron-sulfur (Ip) subunit of succinate dehydrogenase (SDH, EC 1.3.99.1) complex was cloned from Mortierella alpina 1S-4. The deduced amino acid sequence of SdhB from M. alpina 1S-4 showed high similarity to those of SdhB from
Y N Yin et al.
Phytopathology, 101(8), 986-995 (2011-04-08)
Botrytis cinerea isolates obtained from apple orchards were screened for resistance to boscalid. Boscalid-resistant (BosR) isolates were classified into four phenotypes based on the levels of the concentration that inhibited fungal growth by 50% relative to control. Of the 220
Marina DellaGreca et al.
Journal of agricultural and food chemistry, 52(20), 6228-6232 (2004-09-30)
Sunlight exposure of aqueous suspensions of carboxin (1) causes its phototransformation to sulfoxide 2 and minor components. Similar effects are observed in the presence of humic acid or nitrate or at different pH values. Photoproducts 2-9 were isolated by chromatographic
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